Remote Clinical Research Associate – Belgium

Medpace; Belgique; Teletrabalho; USD 74 000 - 102 000; Tempo integral

Resumo da oferta

Medpace is seeking an Experienced Clinical Research Associate to join our Clinical / Country Operations team in Belgium. The role focuses on site visits, regulatory review, and ensuring quality across the study lifecycle.

You will conduct pre-study through closeout visits, verify data, manage drug inventory, and support patient recruitment and safety reporting in a fast‑paced, cross‑functional environment.

Qualificações

• Bachelor of Science in a health-related field is required.
• Previous CRA experience is required.
• Strong knowledge of medical terminology and clinical patient management.
• Basic knowledge of drug therapy techniques and clinical research methodologies.
• Fluent in Dutch, English, and French.

Responsabilidades

• Conduct pre-study, initiation, monitoring, and closeout visits for research sites.
• Perform source document verification and case report form review.
• Perform regulatory document review.
• Conduct study drug inventory.
• Perform adverse event reporting and follow-up.
• Assess patient recruitment and retention.

Conhecimentos

CRA experience

Medical terminology knowledge

Clinical patient management

Drug therapy knowledge

Multilingual: Dutch, English, French

Formação académica

Bachelor of Science in health-related field

Descrição da oferta de emprego

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical / Country Operations team in Belgium. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
• Perform source document verification and case report form review;
• Perform regulatory document review;
• Conduct study drug inventory;
• Perform adverse event and serious adverse event reporting and follow-up; and
• Assess patient recruitment and retention.

Qualifications

• Minimum Bachelor of Science in health-related field;
• Previous experience as a CRA;
• Broad knowledge of medical terminology and clinical patient management;
• Basic knowledge of drug therapy techniques and clinical research methodologies; and
• Excellent command of Dutch, English, and French;

We kindly ask you to send applications in English.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.